(Q35897714)

11 August 2017

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing (English)

1 reference

11 August 2017

1 reference

27

Chris Tyler-Smith

1 reference

11 August 2017

Dongwan Hong

9

0 references

Ryan E. Mills

Ryan E Mills

5

0 references

Young Seok Ju

Young Seok Ju

3

0 references

Omer Gokcumen

Omer Gokcumen

4

0 references

Stephen W. Scherer

25

Stephen W Scherer

1 reference

11 August 2017

Hansoo Park

1

1 reference

11 August 2017

Jong-Il Kim

2

1 reference

11 August 2017

Sheehyun Kim

6

1 reference

11 August 2017

Seungbok Lee

7

1 reference

11 August 2017

Dongwhan Suh

8

1 reference

11 August 2017

Hyunseok Peter Kang

10

1 reference

11 August 2017

Yun Joo Yoo

11

1 reference

11 August 2017

Jong-Yeon Shin

12

1 reference

11 August 2017

Hyun-Jin Kim

13

1 reference

11 August 2017

Maryam Yavartanoo

14

1 reference

11 August 2017

Young Wha Chang

15

1 reference

11 August 2017

Jung-Sook Ha

16

1 reference

11 August 2017

Wilson Chong

17

1 reference

11 August 2017

Ga-Ram Hwang

18

1 reference

11 August 2017

Katayoon Darvishi

19

1 reference

11 August 2017

Hyeran Kim

20

1 reference

11 August 2017

Song Ju Yang

21

1 reference

11 August 2017

Kap-Seok Yang

22

1 reference

11 August 2017

Hyungtae Kim

23

1 reference

11 August 2017

Matthew E Hurles

24

1 reference

11 August 2017

Nigel P Carter

26

1 reference

11 August 2017

Charles Lee

28

1 reference

11 August 2017

Jeong-Sun Seo

29

1 reference

11 August 2017

language of work or name

English

0 references

publication date

4 April 2010

1 reference

11 August 2017

1 reference

11 August 2017

42

1 reference

11 August 2017

400-405

1 reference

11 August 2017

5

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.555

11 August 2017

0 references

cites work

Origins and functional impact of copy number variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

A highly annotated whole-genome sequence of a Korean individual

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Mapping and sequencing of structural variation from eight human genomes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

The fine-scale and complex architecture of human copy-number variation

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Proportionally more deleterious genetic variation in European than in African populations.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Paired-end mapping reveals extensive structural variation in the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Obesity and diabetes in the developing world--a growing challenge

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Global variation in copy number in the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Body-mass index and mortality in Korean men and women.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Putative association between a new polymorphism in exon 3 (Arg109Cys) of the pancreatic colipase gene and type 2 diabetes mellitus in two independent Caucasian study populations

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Fine-scale structural variation of the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Detection of large-scale variation in the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

High frequency of mutations of the PIK3CA gene in human cancers

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Association of LY9 in UK and Canadian SLE families

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

Detection of RhD(el) in RhD-negative persons in clinical laboratory.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

PIK3CA gene is frequently mutated in breast carcinomas and hepatocellular carcinomas.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

The importance of race and ethnic background in biomedical research and clinical practice

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329635

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

24 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.555

A high-resolution survey of deletion polymorphism in the human genome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20364138

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Gastric cancer in Japan

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20364138

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.555

1 reference

Dimensions Publication ID

11 August 2017

0 references

1 reference

11 August 2017

1 reference